Jones Susan
Information and Computational Science Group, The James Hutton Institute, Invergowrie, Dundee, DD2 5DA, UK.
Biophys Rev. 2016 Dec;8(4):359-367. doi: 10.1007/s12551-016-0223-9. Epub 2016 Nov 14.
RNA-binding proteins are functionally diverse within cells, being involved in RNA-metabolism, translation, DNA damage repair, and gene regulation at both the transcriptional and post-transcriptional levels. Much has been learnt about their interactions with RNAs through structure determination techniques and computational modeling. This review gives an overview of the structural data currently available for protein-RNA complexes, and discusses the technical issues facing structural biologists working to solve their structures. The review focuses on three techniques used to solve the 3-dimensional structure of protein-RNA complexes at atomic resolution, namely X-ray crystallography, solution nuclear magnetic resonance (NMR) and cryo-electron microscopy (cryo-EM). The review then focuses on the main computational modeling techniques that use these atomic resolution data: discussing the prediction of RNA-binding sites on unbound proteins, docking proteins, and RNAs, and modeling the molecular dynamics of the systems. In conclusion, the review looks at the future directions this field of research might take.
RNA结合蛋白在细胞内功能多样,参与RNA代谢、翻译、DNA损伤修复以及转录和转录后水平的基因调控。通过结构测定技术和计算建模,人们对它们与RNA的相互作用已经有了很多了解。本综述概述了目前可获得的蛋白质-RNA复合物的结构数据,并讨论了致力于解析其结构的结构生物学家所面临的技术问题。综述重点介绍了用于在原子分辨率下解析蛋白质-RNA复合物三维结构的三种技术,即X射线晶体学、溶液核磁共振(NMR)和冷冻电子显微镜(cryo-EM)。然后,综述重点介绍了使用这些原子分辨率数据的主要计算建模技术:讨论未结合蛋白质上RNA结合位点的预测、蛋白质与RNA的对接以及系统的分子动力学建模。总之,综述展望了该研究领域未来可能的发展方向。